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Addddrreessss ffoorr ccoorrrreessppoonnddeennccee:: Beata Cudowska MD, PhD, University Children’s Teaching Hospital, 17 Waszyngtona St, 15-274 Bialystok, Poland, phone: +48 857 450 710, e-mail: becud@wp.pl
RReecceeiivveedd:: 3.09.2012, aacccceepptteedd:: 28.02.2013.
Supplementation with long chain polyunsaturated fatty acids in treatment of atopic dermatitis in children
Maciej Kaczmarski1, Beata Cudowska2, Małgorzata Sawicka-Żukowska3, Anna Bobrus-Chociej1
1Department of Pediatrics, Gastroenterology and Allergology, Medical University of Bialystok, Poland Head: Prof. Maciej Kaczmarski MD, PhD
2University Children’s Teaching Hospital, Bialystok, Poland Head: Janusz Pomaski MD, PhD
3Department of Pediatric Oncology and Hematology, Medical University of Bialystok, Poland Head: Prof. Maryna Krawczuk-Rybak MD, PhD
Postep Derm Alergol 2013; XXX, 2: 103–107 DOI: 10.5114/pdia.2013.34160
Abstract
Some recent studies indicate that unsaturated fatty acids, components of cellular membranes and precursors of immunomodulators, play a significant role in the pathogenesis of some symptoms of atopic dermatitis. Since they cannot be synthesized by the human body, they must be provided with nutrition as the so called exogenous fatty acids: linoleic (a precursor of arachidonic acid) and α-linolenic acid (a precursor of eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA)). Their deficiency facilitates the development of some disorders, e.g. of the cardio- vascular system or of the nervous system, or becomes the cause of intensification of ailments in their course e.g.
pruritus and dryness in atopic dermatitis. Though clinical examinations to date confirm the efficacy of fatty acid supplementation in treatment of atopic dermatitis, their results are not explicit.
K
Keeyy wwoorrddss:: atopic dermatitis, polyunsaturated fatty acids.
Introduction
The significance of lipids as a natural source of ener- gy, lipid-soluble vitamines and fatty acids, being struc- tural material synthesizing numerous biologically active compounds vital for the human organism, has been the subject of research for many years. Fatty acids are found in vegetable and animal fats and provided with food as, the so called exogenous fatty acids: linoleic (a precursor of arachidonic acid (AA)) and α-linolenic acid (a precur- sor of eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA)) [1]. Ω-3 fatty acids found in oil and fish meat and ω-6 fatty acids obtained from seeds play a signifi- cant role in the organism. They maintain an appropriate structure, elasticity and functioning of cellular membranes as well as are essential in the synthesis of intracellular lipids in the corneous layer of epidermis. Additionally, they are also precursors of eicosanoids and have regulative properties [2]. The supply of these acids in a diet, espe- cially the ratio of saturated acids to monounsaturated and polyunsaturated acids, decides about appropriate functioning of the human body [3]. The examinations
prove that deficiency of unsaturated fatty acids facilitates the development of some disorders, e.g. of the cardio- vascular system or cause the intensification of ailments in their course, e.g. in atopic dermatitis (AD) [2-6].
The results of clinical studies indicate that skin dry- ness, a basic therapeutic problem in AD, is caused mainly by the damage to the protective barrier of the epidermis, which consists of the aqueous and the lipid coat of der- mis, a natural moisturizing factor and intracellular sub- stance of the corneous layer of epidermis [2, 7]. This aile- ment frequently results from the insufficient supply of fatty acids in a diet. The clinical examinations carried out so far reveal that supplementation with preparations of fatty acids gives an opportunity to alleviate the symptoms of the disease and decrease the frequency of intensification of skin lesions in the course of AD [2, 5, 8].
Atopic dermatitis as a chronic inflammatory disease
Atopic dermatitis is a chronic inflammatory skin dis- ease associated, among others, with oversensitivity to
various allergens and environmental agents. The first skin lesions usually appear in the early childhood; however, they can persist and/or appear also in the adult life.
Recently the prevalence of the disease has tended to increase and it occurs in about 10-20% of children and in 1-3% of adults. In many cases, AD lesions appearing in childhood can be the first step of ‘an allergic march’ and prognose allergic rhinitis and bronchial asthma, devel- oping later in the adulthood [9-11].
A clinical manifestation of skin lesions is conditioned by genetic, environmental and immunological factors.
Numerous examinations in vitro and in vivo confirm com- plex etiology of this disease, in which development and complicated immune mechanisms, including numerous cells and cytokines, are involved. Lymphocytes Th2, inter- leukins 4, 5, 13 (IL-4, IL-5, IL-13) and interferon-γ (IFN-γ) play a special role in the development of this disease. The infiltrate of activated memory cells T CD4+ was proved in the analyses of skin bioptates with acute AD lesions, man- ifesting themselves as lichenization, reddening, pruritus, excoriations and exudates. Significantly more cells with the expression of mRNA IL-4, 5 and 13 were proved in the skin of patients with intensified lesions of the AD type in comparison with the skin of healthy subjects. In the skin subjected to long-term inflammation, remodeling takes place, resulting in lichenization, dryness of the marked intensity and the development of fibrous papules. Langer- hans cells predominate in the skin infiltrate, though eosinophiles and lymphocytes T are also present. Marked- ly more cells, expressing mRNA IL-5 and IFN-γ, were found at a low expression of IL-4 and IL-13. In 80% of cases, immune mechanisms of the disease were connected with the IgE-dependent reaction; in about 20% – the IgE-inde- pendent reaction [9, 12, 13].
The opinion that skin lesions resulted mainly from functioning disorders of the immune system and the change in the balance between lymphocyte populations Th2 and Th1/Th0 has predominated for many years. It was regarded that this caused the development of the IgE- dependent oversensitivity to airborne and food allergens (type I allergic reaction) in the acute phase of the disease.
These phenomena were supposed to be responsible for the development of inflammatory changes within the der- mis and epidermis (the so-called ‘inside’ theory). In recent years, studies have shown a genetically-conditioned dys- function of the epidermal barrier associated with abnor- mal synthesis of structural proteins, high concentration of proteases and low activity of their inhibitors. Disorders of the epidermal barrier function, enabling allergens and irritating environmental agents to penetrate, are regard- ed as the primary factor in the etiopathogenesis of atopic eczema (the ‘outside’ theory) [7].
Lately, functional disorders of filaggrin, one of the key proteins conditioning a normal barrier function of the epi- dermis, have become the focus of researchers’ attention.
This function can be disturbed due to the mutation in the
gene encoding filaggrin. The most frequently described mutations are R501X and 2282del4, predisposing, espe- cially, to eczema lesions of an early onset as well as the severe and chronic course in patients with co-existing atopy [14].
Normal functioning of the epidermal barrier and, most of all, its hydration is associated with the metabolism of fatty acids and the appropriate supply of linolenic acid in a diet [2, 12].
TThhee rroollee ooff lloonngg--cchhaaiinn ppoollyyuunnssaattuurraatteedd ffaattttyy aacciiddss ((LLCCPPUUFFAAss)) aanndd mmeettaabboolliitteess ooff aarraacchhiiddoonniicc aacciidd iinn tthhee ppaatthhooggeenneessiiss ooff aattooppiicc ddeerrmmaattiittiiss
Recent studies indicate that fatty acids, components of cellular membranes and precursors of immunomodu- lators, play a significant role in the pathogenesis of atopic dermatitis. They are built into e.g. ceramides and metab- olized to various metabolites in the dermis due to lypo- and cyclooxygenase. A detailed mechanism of their activ- ity has not been explained so far since the majority of studies refer to adults and some findings are contradic- tive [12].
Ω-3 and ω-6 acids, whose names come from the loca- tion of double binds counting from the end of the carbon chain, can be distinguished out of LC-PUFA. The synthe- sis of long-chain polyunsaturated fatty acids is conduct- ed via two pathways. The former initiates the metabolism of linoleic acid (LA, 18:2 n-6) and leads to the formation of arachidonic acid (AA), and next prostaglandins, leu - kotrienes and thromboxanes; the latter – α-linolenic acid (ALA, 18:3 n-3), leading to the synthesis of eicosapen- taenoic acid (EPA, 20:5 n-3) and docosahexaenoic acid (DHA 22:6 n-3). The same enzymes, desaturases (∆-5 and
∆-6) and elongases, whose accurate functioning is of basic importance in the metabolism of LCPUFA, take part in both LA and AA transformations. The final products of the line n-6 metabolism have the proinflammatory, iatrogenic activity and they enhance cell proliferation. Metabolites of the line n-3 oppose these unfavorable activities, decreasing the intensity of an inflammatory process and platelet aggregation, protecting the endothelium and blood vessels, reducing the level of antioxidative stress, insulin sensitivity and improving a lipid profile. The EPA is regarded as the main anti-inflammatory factor due to its competitive activity with AA for metabolites. Howev- er, it has also been proved that DHA shows a potent anti- inflammatory and immunomodulating activity [8, 12, 15].
In 1929, in the experimental animal studies, Burr et al. proved the relation between skin lesions, charac- terized by excessive dryness, reddening and the presence of abnormal keranocytes, and a deficit of LCPUFAs in a diet. The above abnormalities initially found in animals were also observed in humans. Children on cow’s milk preparations, poor in fatty acids, demonstrated inflam- matory skin lesions. Deficiency in LA caused dryness, red-
dening and pruritus, leading to skin disorders. The increased index of endothelial cell proliferation, enhanced metabolism with an increase in the synthesis of sterol esters and then the presence of abnormal keratynocytes were found in histopathological examinations of skin biopatates.
In 1937, Brown and Hansen proved the decreased con- centration of AA in the serum of children with atopic der- matitis, whereas the abnormal fatty acids profile and the decreased activity of ∆-6-desaturase, an enzyme taking part in denaturation of LA to γ-linolenic acid (GLA), have been recently found in these patients. The GLA is a pre- cursor of proinflammatory and immunomodulating agents, such as leukotrienes and prostaglandin E1, which is involved in maturation and differentiation of lympho- cytes T, thus influencing the IgE production [8, 12].
A moderately increased concentration of LA and a sig- nificantly decreased concentration of AA and DHA were reported in a Swedish study carried out in children with AD. Additionally, a positive correlation was proved between the concentration of immunoglobulin E in the umbilical blood and the concentration of LA. The hypothesis was put forward that an increased risk of AD development could be caused by disorders of LA metabolism [12].
In other studies carried out as early as in the middle of the last century by Hansen et al., the decreased con- centration of LA metabolites with the increased concen- tration of the acid in the blood serum was found in moth- ers breastfeeding infants with AD, compared to healthy infants’ mothers [16]. The above findings were also con- firmed by contemporary studies [17, 18]. Their analysis shows that the decreased conversion of LA to its metabo- lites and the likely decreased building-in of fatty acids to phospholipids are observed in patients with AD. These abnormalities cause a decrease in the synthesis of prostaglandin E1 (PGE1), resulting in a low concentration of cAMP, which in consequence leads to the activation of specific structures of the immune system [17, 18].
None of the above studies enabled to answer the question whether the changes in fatty acids metabolism were the cause or consequence of atopic dermatitis. Pub- lished in 1994, Galli et al.’s studies determined the metabolites of fatty acids metabolism in the umbilical blood of children from the families with a positive histo- ry of atopic diseases and proved that changes in the metabolism of fatty acids caused no skin lesions [12, 19].
In the last ten years, much attention was paid to the studies of the genetic background of differences in the metabolism of LC-PUFA and disorders of the ∆-6 desat- urase activity [7]. To date, evaluating the fatty tissue, breast milk, umbilical blood and lymphocytes of the umbilical blood, fibroblasts and erythrocytes, the abnormal metab- olism of fatty acids, involving a decreased concentration of LA metabolites, especially, GLA and AA at a normal con- centration of LA, were proved in patients with AD [8, 20].
SSiiggnniiffiiccaannccee ooff ssuupppplleemmeennttaattiioonn wwiitthh pprreeppaarraattiioonnss ooff γγ--lliinnoolleenniicc aacciidd iinn tthhee ttrreeaattmmeenntt ooff aattooppiicc ddeerrmmaattiittiiss
Long-chain polyunsaturated fatty acids are indispen- sible components of a diet because they cannot be syn- thesized by the human organism. The source of n-3 acids in a diet is mainly sea fish (herring, salmon, trout and oth- ers), sea food and oils (linen, rape-seed) and walnuts, whereas the main source of n-6 acids is corn, arachidic, cotton, soya and sesame oils, olive oil and plant seeds.
Even in the case of a sufficient supply of linoleic and LA, this supplementation may be insufficient to synthesize the appropriate amount of LCPUFAs. This synthesis depends on the age, accompanying genetic and environ- mental conditions, etc. Poland is the country where defi- ciency of polyunsaturated fatty acids in a diet is especially high. Fish consumption in the adult population is insuffi- cient and constitutes about 50% of the recommended consumption, whereas an average Pole provides his/her organism with approximately 1/5 of demand for neces- sary fatty acids [1, 2, 4, 21].
Numerous studies performed on animal models and in people prove a favorable influence of the diet rich in polyunsaturated fatty acids in many diseases (e.g. car- diovascular, neurological, psychiatric, endocrinological, ophthalmological, dermatological or allergic diseases) [1, 4, 22]. More and more examinations confirm a positive effect of long-term supplementation with LC-PUFA in infancy on the development of the central nervous sys- tem [21].
The influence of polyunsaturated fatty acids on the development of diseases with allergic etiology has been examined numerous times as early as in the prenatal peri- od. The anti-allergic activity of LC-PUFA has been analysed mostly in patients with bronchial asthma and AD [2, 12, 13, 23]. It has been proved that if a diet is abundant in GLA, an increase in its metabolites: PGE1 and 15-hydroxy- eicozatrienoic acid with anti-inflammatory activity is found in the dermis.
Additionally, it has been found that supplementation with preparations of fatty acids during pregnancy leads to a decreased incidence and intensity of AD in children [24-26]. A detailed mechanism of the anti-allergic activi- ty of LC-PUFA acids in AD has not been explained com- pletely. The first findings on a favorable influence of fat- ty acids on the animal and human skin with AD come from the 1930s [16]. For the next decades, various prepa- rations containing LC-PUFA were used to treat this dis- ease, especially, those containing compounds with the various content of LA and GLA, usually improving the skin condition [23, 27]. Ω-3 and ω-6 fatty acids provide the appropriate structure, elasticity and functionality of cell membranes and are vital for the synthesis of intracellu- lar lipids in the corneous layer in the epithelium.
In the 1980s, more and more findings on supplemen- tation with GLA preparations in the form of primrose oil
(EPO), which contains 72% of LA and 9% of GLA, were published [12]. So far, many data containing various clin- ical experiments have been issued with only one sys- tematic review of the literature on this subject. This meta- analysis dated 1989, which contained both published and unpublished data, is criticized for lack of detailed criteria with regard to unpublished data. It referred to the ran- domized studies and oral supplementation with fatty acids and did not confirm a favorable effect of such man- agement on the severity of AD. According to authors, the efficacy, observed in some groups of patients, e.g. in infants and patients with severe AD, did not prove the need for or abandonment of this treatment [24, 28]. Sim- ilarly, a new meta-analysis, made in 2004, did not con- firm a significant influence of GLA on the severity of AD [27]. The exception was a positive influence of fish oil on skin peeling and dryness.
However, a significant advantage of this preparation was found in other clinical randomized examinations per- formed by Schalin-Karrila et al. The amount of steroids applied topically was an important indicator of efficacy. It was observed that children treated with placebo used three times more steroid ointments than those treated with EPO [29]. Positive results were also demonstrated in a study by Biagi et al., who additionally found that this favorable effect lasted for a long time [30].
Dunstan et al. evaluated the influence of oral supple- mentation with preparations of fish oils in pregnant women suffering from atopic dermatitis, on the content of IgA, CD14, some cytokines (IL-5, IL-6, IL-10, TNF-α, IFN-γ) and fatty acids in the breast milk after delivery.
A significantly higher concentration of EPA and DHA was revealed in the milk of women taking preparations of fat- ty acids during pregnancy in comparison with controls.
Additionally, it was proved that the course of AD in chil- dren of these mothers was milder [31].
Galli et al. suggest that the supplementation with GLA plays a significant role in the early stage of AD develop- ment, therefore administration of preparations of these acids seems extremely purposeful in the early childhood.
Steward et al. claim that EPO changes slowly and gradu- ally the composition of lipids in the cell membranes to the appropriate level [2].
Published in 2012, randomized examinations investi- gating the effect of supplementation with ω-3 acids in pregnant women on the incidence of allergy in children, did not confirm a favorable influence of such manage- ment on the value of the total IgE concentration in the study group. A less frequent incidence of AD and sensi- tivity to hen’s egg albumin was observed among children of mothers using supplementation with ω-3 acids during pregnancy [23]. In other clinical studies with the same intervention, a decrease in the concentration of AA and an increase in the ratio of EPA to DHA were revealed in the blood serum of women using supplementation with preparations of ω-3 acid [32].
According to the opinion of the Experts’ Group, pub- lished in 2011, pregnant and breastfeeding women should be supplemented with min. 200 mg of DHA daily, where- as children above the age of 3 are recommended to con- sume long-chain fatty acids ω-3 at a dose of 150-200 mg in 24 h [5].
At present, in the market there are numerous prepa- rations containing acids from the ω-3 group, though not all of them contain the appropriate dosage of these acids, taking into consideration their marked deficiency in a diet [2]. Polyunsaturated fatty acids are safe supplements of a diet, because they induce occasional, transitional and insignificant clinical side effects, usually, of the dyspep- tic character. The DHA, whose activity was confirmed in numerous studies, including populations of healthy and ill people at various ages, seems to be the safest. The EPA, via its competition with AA, has some limitations when administered in infants (impaired growth). During exclu- sive breast feeding, the first 6 months of life, an additional intake of DHA seems not to be advised, because breast milk provides sufficient supplementation. The supple- mentation of feeding should be initiated after this peri- od, introducing an additional source of ω-3 acids e.g. fish into the diet [2]. Treatment of children with AD is multi- directed with an elimination of agalactic, hypoallergic diet, in which it is not advisable to consume sea fish, nuts – a rich source of LC-PUFA acids as well as strong allergens.
Thus, these patients are additionally at risk of an insuffi- cient intake of these acids and their supplementation in a diet is especially significant.
Conclusions
Based on available meta-analyses, it can be assumed that efficacy of supplementation with EFA in the treat- ment of AD is not completely documented. A positive effect of using these preparations in some age groups e.g.
in AD children up to 1 year old can be observed, however the studies published so far neither confirm nor deny this thesis. Thus, it is advisable to conduct clinical studies aimed at proving a different influence of various fatty acids on the concentration of proinflammatory cytokines in children with atopic dermatitis. The confirmation of the immunological modulation by polyunsaturated fatty acids in these patients could help to decide whether it is nec- essary to introduce the accessory therapy of LC-PUFA acids in AD treatment. The improved condition of the skin, decreased incidence of AD lesions and alleviated ailments like pruritus, could improve the quality of life of these chil- dren and their parents as well as this would have favor- able financial results.
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